Dhvar5- and MSI78-coated titanium are bactericidal against methicillin-resistant Staphylococcus aureus, immunomodulatory and osteogenic

Detalhes bibliográficos
Autor(a) principal: Costa, B.
Data de Publicação: 2025
Outros Autores: Coelho, J., Silva, V., Shahrour, H., Costa, N. A. [UNESP], Ribeiro, A. R., Santos, S. G., Costa, F., Martínez-de-Tejada, G., Monteiro, C., Martins, M. C.L.
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNESP
Texto Completo: http://dx.doi.org/10.1016/j.actbio.2024.11.016
https://hdl.handle.net/11449/307770
Resumo: Infection is one of the major issues associated with the failure of orthopedic devices, mainly due to implant bacterial colonization, biofilm formation, and associated antibiotic resistance. Antimicrobial peptides (AMP) are a promising alternative to conventional antibiotics given their broad-spectrum of activity, low propensity to induce bacterial resistance, and ability to modulate host immune responses. Dhvar5 (LLLFLLKKRKKRKY) and MSI78 (GIGKFLKKAKKFGKAFVKILKK) are two AMP with broad-spectrum activity against bacteria, including methicillin-resistant Staphylococcus aureus (MRSA), one of the most problematic etiologic agents in Orthopedic Devices-Related Infections (ODRI). This work aims to evaluate the bactericidal, immunomodulatory and osteogenic potential of Dhvar5- and MSI78-coated titanium surfaces (AMP-Ti). Two AMP-Ti surfaces were successfully obtained by grafting Dhvar5 (0.8 ± 0.1 µM/mm2) or MSI78 (0.5 ± 0.3 µM/mm2) onto titanium substrates through a polydopamine layer. Both AMP-Ti were bactericidal against MRSA, eradicating bacteria upon contact for 6 h in a culture medium supplemented with human plasma proteins. The AMP-Ti immunomodulatory potential was evaluated using human primary macrophages, by assessing surfaces capacity to induce pro-/anti-inflammatory (M1/M2) markers and cytokines. While in naïve conditions both AMP-Ti surfaces slightly promoted the M2 marker CD163, in response to LPS and IFN-γ (simulating a bacterial infection), both AMP increased the M1 marker CCR7 and enhanced macrophage secretion of pro-inflammatory IL-6 and TNF-α cytokines, particularly for Ti-MSI78 surfaces. Additionally, both AMP-Ti surfaces were cytocompatible and promoted osteoblastic cell differentiation. This proof-of-concept study demonstrated the high potential of Dhvar5- and MSI78-Ti as antimicrobial coatings for ODRI prevention. Statement of significance: This study investigates the bactericidal effects of the antimicrobial peptides Dhvar5 and MSI78, immobilized on titanium (Ti) surfaces through a polydopamine coating, aiming at the prevention of Orthopedic-Device Related Infections (ODRIs). The developed coatings displayed MRSA-sterilizing activity, while revealing an immunomodulatory potential towards macrophages and promoting osteoblastic cell differentiation. This strategy allows a quick and easy immobilization of high quantities of AMP, unlike most other approaches, thus favoring its clinical translation.
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spelling Dhvar5- and MSI78-coated titanium are bactericidal against methicillin-resistant Staphylococcus aureus, immunomodulatory and osteogenicAntibacterial activityAntimicrobial peptidesDopamineImmunomodulationMacrophagesSurface immobilizationInfection is one of the major issues associated with the failure of orthopedic devices, mainly due to implant bacterial colonization, biofilm formation, and associated antibiotic resistance. Antimicrobial peptides (AMP) are a promising alternative to conventional antibiotics given their broad-spectrum of activity, low propensity to induce bacterial resistance, and ability to modulate host immune responses. Dhvar5 (LLLFLLKKRKKRKY) and MSI78 (GIGKFLKKAKKFGKAFVKILKK) are two AMP with broad-spectrum activity against bacteria, including methicillin-resistant Staphylococcus aureus (MRSA), one of the most problematic etiologic agents in Orthopedic Devices-Related Infections (ODRI). This work aims to evaluate the bactericidal, immunomodulatory and osteogenic potential of Dhvar5- and MSI78-coated titanium surfaces (AMP-Ti). Two AMP-Ti surfaces were successfully obtained by grafting Dhvar5 (0.8 ± 0.1 µM/mm2) or MSI78 (0.5 ± 0.3 µM/mm2) onto titanium substrates through a polydopamine layer. Both AMP-Ti were bactericidal against MRSA, eradicating bacteria upon contact for 6 h in a culture medium supplemented with human plasma proteins. The AMP-Ti immunomodulatory potential was evaluated using human primary macrophages, by assessing surfaces capacity to induce pro-/anti-inflammatory (M1/M2) markers and cytokines. While in naïve conditions both AMP-Ti surfaces slightly promoted the M2 marker CD163, in response to LPS and IFN-γ (simulating a bacterial infection), both AMP increased the M1 marker CCR7 and enhanced macrophage secretion of pro-inflammatory IL-6 and TNF-α cytokines, particularly for Ti-MSI78 surfaces. Additionally, both AMP-Ti surfaces were cytocompatible and promoted osteoblastic cell differentiation. This proof-of-concept study demonstrated the high potential of Dhvar5- and MSI78-Ti as antimicrobial coatings for ODRI prevention. Statement of significance: This study investigates the bactericidal effects of the antimicrobial peptides Dhvar5 and MSI78, immobilized on titanium (Ti) surfaces through a polydopamine coating, aiming at the prevention of Orthopedic-Device Related Infections (ODRIs). The developed coatings displayed MRSA-sterilizing activity, while revealing an immunomodulatory potential towards macrophages and promoting osteoblastic cell differentiation. This strategy allows a quick and easy immobilization of high quantities of AMP, unlike most other approaches, thus favoring its clinical translation.i3S – Instituto de Investigação e Inovação em Saúde Universidade do PortoINEB – Instituto de Engenharia Biomédica Universidade do PortoFEUP–Faculdade de Engenharia Universidade do PortoICBAS – Instituto de Ciências Biomédicas Abel Salazar Universidade do PortoColégio Internato dos Carvalhos (CIC)Department of Microbiology and Parasitology University of NavarraNavarra Institute for Health Research (IdiSNA)UNESP - Universidade Estadual Paulista Faculdade de Ciências, SPNanoSafety Group International Iberian Nanotechnology LaboratoryUNESP - Universidade Estadual Paulista Faculdade de Ciências, SPUniversidade do PortoColégio Internato dos Carvalhos (CIC)University of NavarraNavarra Institute for Health Research (IdiSNA)Universidade Estadual Paulista (UNESP)International Iberian Nanotechnology LaboratoryCosta, B.Coelho, J.Silva, V.Shahrour, H.Costa, N. A. [UNESP]Ribeiro, A. R.Santos, S. G.Costa, F.Martínez-de-Tejada, G.Monteiro, C.Martins, M. C.L.2025-04-29T20:10:17Z2025-01-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article98-112http://dx.doi.org/10.1016/j.actbio.2024.11.016Acta Biomaterialia, v. 191, p. 98-112.1878-75681742-7061https://hdl.handle.net/11449/30777010.1016/j.actbio.2024.11.0162-s2.0-85209664352Scopusreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengActa Biomaterialiainfo:eu-repo/semantics/openAccess2025-04-30T13:56:45Zoai:repositorio.unesp.br:11449/307770Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestrepositoriounesp@unesp.bropendoar:29462025-04-30T13:56:45Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false
dc.title.none.fl_str_mv Dhvar5- and MSI78-coated titanium are bactericidal against methicillin-resistant Staphylococcus aureus, immunomodulatory and osteogenic
title Dhvar5- and MSI78-coated titanium are bactericidal against methicillin-resistant Staphylococcus aureus, immunomodulatory and osteogenic
spellingShingle Dhvar5- and MSI78-coated titanium are bactericidal against methicillin-resistant Staphylococcus aureus, immunomodulatory and osteogenic
Costa, B.
Antibacterial activity
Antimicrobial peptides
Dopamine
Immunomodulation
Macrophages
Surface immobilization
title_short Dhvar5- and MSI78-coated titanium are bactericidal against methicillin-resistant Staphylococcus aureus, immunomodulatory and osteogenic
title_full Dhvar5- and MSI78-coated titanium are bactericidal against methicillin-resistant Staphylococcus aureus, immunomodulatory and osteogenic
title_fullStr Dhvar5- and MSI78-coated titanium are bactericidal against methicillin-resistant Staphylococcus aureus, immunomodulatory and osteogenic
title_full_unstemmed Dhvar5- and MSI78-coated titanium are bactericidal against methicillin-resistant Staphylococcus aureus, immunomodulatory and osteogenic
title_sort Dhvar5- and MSI78-coated titanium are bactericidal against methicillin-resistant Staphylococcus aureus, immunomodulatory and osteogenic
author Costa, B.
author_facet Costa, B.
Coelho, J.
Silva, V.
Shahrour, H.
Costa, N. A. [UNESP]
Ribeiro, A. R.
Santos, S. G.
Costa, F.
Martínez-de-Tejada, G.
Monteiro, C.
Martins, M. C.L.
author_role author
author2 Coelho, J.
Silva, V.
Shahrour, H.
Costa, N. A. [UNESP]
Ribeiro, A. R.
Santos, S. G.
Costa, F.
Martínez-de-Tejada, G.
Monteiro, C.
Martins, M. C.L.
author2_role author
author
author
author
author
author
author
author
author
author
dc.contributor.none.fl_str_mv Universidade do Porto
Colégio Internato dos Carvalhos (CIC)
University of Navarra
Navarra Institute for Health Research (IdiSNA)
Universidade Estadual Paulista (UNESP)
International Iberian Nanotechnology Laboratory
dc.contributor.author.fl_str_mv Costa, B.
Coelho, J.
Silva, V.
Shahrour, H.
Costa, N. A. [UNESP]
Ribeiro, A. R.
Santos, S. G.
Costa, F.
Martínez-de-Tejada, G.
Monteiro, C.
Martins, M. C.L.
dc.subject.por.fl_str_mv Antibacterial activity
Antimicrobial peptides
Dopamine
Immunomodulation
Macrophages
Surface immobilization
topic Antibacterial activity
Antimicrobial peptides
Dopamine
Immunomodulation
Macrophages
Surface immobilization
description Infection is one of the major issues associated with the failure of orthopedic devices, mainly due to implant bacterial colonization, biofilm formation, and associated antibiotic resistance. Antimicrobial peptides (AMP) are a promising alternative to conventional antibiotics given their broad-spectrum of activity, low propensity to induce bacterial resistance, and ability to modulate host immune responses. Dhvar5 (LLLFLLKKRKKRKY) and MSI78 (GIGKFLKKAKKFGKAFVKILKK) are two AMP with broad-spectrum activity against bacteria, including methicillin-resistant Staphylococcus aureus (MRSA), one of the most problematic etiologic agents in Orthopedic Devices-Related Infections (ODRI). This work aims to evaluate the bactericidal, immunomodulatory and osteogenic potential of Dhvar5- and MSI78-coated titanium surfaces (AMP-Ti). Two AMP-Ti surfaces were successfully obtained by grafting Dhvar5 (0.8 ± 0.1 µM/mm2) or MSI78 (0.5 ± 0.3 µM/mm2) onto titanium substrates through a polydopamine layer. Both AMP-Ti were bactericidal against MRSA, eradicating bacteria upon contact for 6 h in a culture medium supplemented with human plasma proteins. The AMP-Ti immunomodulatory potential was evaluated using human primary macrophages, by assessing surfaces capacity to induce pro-/anti-inflammatory (M1/M2) markers and cytokines. While in naïve conditions both AMP-Ti surfaces slightly promoted the M2 marker CD163, in response to LPS and IFN-γ (simulating a bacterial infection), both AMP increased the M1 marker CCR7 and enhanced macrophage secretion of pro-inflammatory IL-6 and TNF-α cytokines, particularly for Ti-MSI78 surfaces. Additionally, both AMP-Ti surfaces were cytocompatible and promoted osteoblastic cell differentiation. This proof-of-concept study demonstrated the high potential of Dhvar5- and MSI78-Ti as antimicrobial coatings for ODRI prevention. Statement of significance: This study investigates the bactericidal effects of the antimicrobial peptides Dhvar5 and MSI78, immobilized on titanium (Ti) surfaces through a polydopamine coating, aiming at the prevention of Orthopedic-Device Related Infections (ODRIs). The developed coatings displayed MRSA-sterilizing activity, while revealing an immunomodulatory potential towards macrophages and promoting osteoblastic cell differentiation. This strategy allows a quick and easy immobilization of high quantities of AMP, unlike most other approaches, thus favoring its clinical translation.
publishDate 2025
dc.date.none.fl_str_mv 2025-04-29T20:10:17Z
2025-01-01
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://dx.doi.org/10.1016/j.actbio.2024.11.016
Acta Biomaterialia, v. 191, p. 98-112.
1878-7568
1742-7061
https://hdl.handle.net/11449/307770
10.1016/j.actbio.2024.11.016
2-s2.0-85209664352
url http://dx.doi.org/10.1016/j.actbio.2024.11.016
https://hdl.handle.net/11449/307770
identifier_str_mv Acta Biomaterialia, v. 191, p. 98-112.
1878-7568
1742-7061
10.1016/j.actbio.2024.11.016
2-s2.0-85209664352
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Acta Biomaterialia
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 98-112
dc.source.none.fl_str_mv Scopus
reponame:Repositório Institucional da UNESP
instname:Universidade Estadual Paulista (UNESP)
instacron:UNESP
instname_str Universidade Estadual Paulista (UNESP)
instacron_str UNESP
institution UNESP
reponame_str Repositório Institucional da UNESP
collection Repositório Institucional da UNESP
repository.name.fl_str_mv Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)
repository.mail.fl_str_mv repositoriounesp@unesp.br
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